US11125760B2ActiveUtilityA1

Methods and compositions for diagnosing and treating loss and/or distortion of taste or smell

Assignee: CYRANO THERAPEUTICS INCPriority: Feb 18, 2014Filed: Dec 23, 2019Granted: Sep 21, 2021
Est. expiryFeb 18, 2034(~7.6 yrs left)· nominal 20-yr term from priority
A61K 31/658A61K 31/197A61K 31/44A61P 27/00A61K 31/5575A61K 45/06G01N 33/6893A61K 31/506A61K 31/4709A61K 38/26A61K 9/0043A61K 31/5377A61K 31/522A61K 2300/00A61K 31/352
93
PatentIndex Score
5
Cited by
275
References
23
Claims

Abstract

Disclosed herein are methods for diagnosing a subject with loss and/or distortion of taste or smell, e.g., hyposmia, dysosmia, anosmia, phantosmia, hypogeusia, dysgeusia, phantogeusia, and/or ageusia. Also disclosed herein are methods and compositions for treating a subject for loss and/or distortion of taste or smell, e.g., hyposmia, dysosmia, anosmia, phantosmia, hypogeusia, dysgeusia, phantogeusia, and/or ageusia.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method of treating a taste or smell disorder, comprising administering to a subject having the taste or smell disorder a pharmaceutical composition comprising a PDE inhibitor, wherein the administering is sufficient to increase a level of sonic hedgehog (SHH) in nasal mucus or saliva of the subject by at least about 10%, relative to a level of SHH prior to the administering. 
     
     
       2. The method of  claim 1 , wherein the pharmaceutical composition has a pH of from about 6 to about 8, wherein about is plus or minus 10%. 
     
     
       3. The method of  claim 1 , wherein the subject is a female. 
     
     
       4. The method of  claim 1 , wherein the administering is sufficient to decrease an H value for pyridine or thiophene, relative to an H value for pyridine or thiophene prior to the administering. 
     
     
       5. The method of  claim 1 , wherein the administering is sufficient to decrease an H value for pyridine or thiophene, relative to an H value for pyridine or thiophene prior to the administering. 
     
     
       6. The method of  claim 1 , wherein the taste or smell disorder comprises hyposmia, dysosmia, anosmia, phantosmia, or a combination thereof. 
     
     
       7. The method of  claim 1 , wherein the PDE inhibitor is a non-selective PDE inhibitor, or a salt thereof. 
     
     
       8. The method of  claim 1 , wherein the PDE inhibitor is a selective PDE inhibitor, or a salt thereof. 
     
     
       9. The method of  claim 8 , wherein the selective PDE inhibitor, or a salt thereof, is a phosphodiesterase-1 selective inhibitor, or a salt thereof; a phosphodiesterase-2 selective inhibitor, or a salt thereof; a phosphodiesterase-3 selective inhibitor, or a salt thereof; a phosphodiesterase-4 selective inhibitor, a phosphodiesterase-5 selective inhibitor, or a salt thereof, a phosphodiesterase-10 selective inhibitor, or a salt thereof; or any combination thereof. 
     
     
       10. The method of  claim 1 , wherein the PDE inhibitor is roflumilast, or a salt thereof cilostazol, or a salt thereof; or any combination thereof. 
     
     
       11. The method of  claim 1 , wherein the PDE inhibitor is theophylline, or a salt thereof. 
     
     
       12. The method of  claim 1 , wherein the administering is intranasal. 
     
     
       13. A method comprising:
 a. measuring a level of sonic hedgehog (SHH) in a biological sample that comprises nasal mucus, saliva, or a combination thereof; 
 b. with the aid of a computer system comprising a computer processor and computer readable memory, identifying a subject as having a taste or smell disorder, wherein the identifying comprises:
 i. comparing a level of SHH in the biological sample a threshold level stored at least transiently on the computer readable memory; 
 ii. detecting a lower level of SHH in the biological sample, relative to the threshold level; and 
 iii. communicating a presence of the taste or smell disorder based on the detecting of (ii). 
 
 
     
     
       14. The method of  claim 13 , further comprising repeating (a) after a time period of about a week after the measuring of (a). 
     
     
       15. The method of  claim 14 , further comprising administering a PDE inhibitor after the identifying of (b). 
     
     
       16. The method of  claim 15 , further comprising monitoring the progression of treatment of the PDE inhibitor, wherein the monitoring comprises:
 performing the identifying of (b) after the administering over the time period of about a week, and repeating the administering if the level of SHH in the biological sample is lower than the threshold level. 
 
     
     
       17. The method of  claim 16 , further comprising terminating the administering of the PDE inhibitor or salt thereof when the level of SHH is in the biological sample is at least 10% higher than the threshold level. 
     
     
       18. The method of  claim 13 , wherein the taste or smell disorder comprises hyposmia, dysosmia, anosmia, phantosmia, or a combination thereof. 
     
     
       19. The method of  claim 15 , wherein the PDE inhibitor is a non-selective PDE inhibitor, or a salt thereof. 
     
     
       20. The method of  claim 15 , wherein the PDE inhibitor is a selective PDE inhibitor, or a salt thereof. 
     
     
       21. The method of  claim 20 , wherein the selective PDE inhibitor, or a salt thereof, is a phosphodiesterase-1 selective inhibitor, or a salt thereof; a phosphodiesterase-2 selective inhibitor, or a salt thereof; a phosphodiesterase-3 selective inhibitor, or a salt thereof; a phosphodiesterase-4 selective inhibitor, a phosphodiesterase-5 selective inhibitor, or a salt thereof, a phosphodiesterase-10 selective inhibitor, or a salt thereof; or any combination thereof. 
     
     
       22. The method of  claim 15 , wherein the PDE inhibitor is roflumilast, or a salt thereof cilostazol, or a salt thereof; or any combination thereof. 
     
     
       23. The method of  claim 15 , wherein the PDE inhibitor is theophylline, or a salt thereof.

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